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AI 根据所提供的论文材料归类:文本研究一般成分数据协方差及微生物依赖结构,未明确涉及经济网络、金融因子或其他所列方向。

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关注这篇论文的作者
Yuanpei Cao
Wei Lin
Hongzhe Li

基于成分调整阈值法的高维成分数据协方差估计

研究问题
当高维观测成分总和受限为一、常规协方差分析可能失效时,如何从成分数据估计潜在基底变量的稀疏协方差结构?
方法与思路
作者提出 COAT,利用成分协方差与基底协方差的分解关系,对样本中心化对数比协方差作阈值处理,并研究高维近似识别。
材料陈述的贡献
摘要称给出可识别性分析、谱范数收敛率和支持恢复保证;模拟中优于部分优化估计器,并用于人体肠道微生物数据。
阅读关注点
应核对基底协方差稀疏假设、近似识别误差、阈值选择、支持恢复条件,以及模拟比较和微生物应用的预处理。
阅读边界
仅据 OpenAlex 摘要,无法确认完整稀疏条件、维度增长限制或改进幅度;成分间依赖也不能直接解释为因果关系。

原文摘要

Yuanpei Caoa, Wei Linb & Hongzhe Lia*a Department of Biostatistics and Epidemiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PAb School of Mathematical Sciences and Center for Statistical Science, Peking University, Beijing, ChinaCONTACT Hongzhe Li hongzhe@upenn.edu Department of Biostatistics and Epidemiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.Color versions of one or more of the figures in the article can be found online at www.tandfonline.com/r/JASA.Supplementary materials for this article are available online. Please go to www.tandfonline.com/r/JASA.ABSTRACTHigh-dimensional compositional data arise naturally in many applications such as metagenomic data analysis. The observed data lie in a high-dimensional simplex, and conventional statistical methods often fail to produce sensible results due to the unit-sum constraint. In this article, we address the problem of covariance estimation for high-dimensional compositional data and introduce a composition-adjusted thresholding (COAT) method under the assumption that the basis covariance matrix is sparse. Our method is based on a decomposition relating the compositional covariance to the basis covariance, which is approximately identifiable as the dimensionality tends to infinity. The resulting procedure can be viewed as thresholding the sample centered log-ratio covariance matrix and hence is scalable for large covariance matrices. We rigorously characterize the identifiability of the covariance parameters, derive rates of convergence under the spectral norm, and provide theoretical guarantees on support recovery. Simulation studies demonstrate that the COAT estimator outperforms some existing optimization-based estimators. We apply the proposed method to the analysis of a microbiome dataset to understand the dependence structure among bacterial taxa in the human gut.

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